Loading...

Loss of matrilin 1 does not exacerbate the skeletal phenotype in a mouse model of multiple epiphyseal dysplasia caused by a Matn3 V194D mutation

OBJECTIVE: Mutations in matrilin 3 can result in multiple epiphyseal dysplasia (MED), a disease characterized by delayed and irregular bone growth and early-onset osteoarthritis. Although intracellular retention of the majority of mutant matrilin 3 was previously observed in a murine model of MED ca...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Main Authors: Bell, Peter A, Piróg, Katarzyna A, Fresquet, Maryline, Thornton, David J, Boot-Handford, Raymond P, Briggs, Michael D
Format: Artigo
Sprog:Inglês
Udgivet: Wiley Subscription Services, Inc., A Wiley Company 2012
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3374853/
https://ncbi.nlm.nih.gov/pubmed/22083516
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/art.33486
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!